Salvage Focal Therapy Via High Intensity Focused Ultrasound (HIFU) in Radiorecurrent Localized Prostate Cancer
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Prostate Cancer
- Sponsor
- University of Florida
- Enrollment
- 25
- Locations
- 1
- Primary Endpoint
- In-field failure-free survival
- Status
- Recruiting
- Last Updated
- 10 months ago
Overview
Brief Summary
This study will investigate the efficacy of focal high intensity focused ultrasound (HIFU) in patients with localized radiorecurrent prostate cancer. This study will also investigate the change in participant quality of life after HIFU therapy as compared to before HIFU therapy.
Detailed Description
Focal therapy is increasingly popular due to its minimal side effect profile. Furthermore, HIFU has demonstrated favorable oncologic outcomes in well selected patients, including those with intermediate and high risk disease. In patients with radiorecurrent prostate cancer there remains a paucity of data on the value of focal therapy. Review of focal HIFU rather than whole gland HIFU is based on largely retrospective data and in an era where mpMRI and PSMA PET was not yet widely implemented thus not reflecting the current patient population seeking this care. In fact, and to the investigators' knowledge, only one study has prospectively evaluated focal HIFU therapy in radiorecurrent prostate cancer. Further evaluation into the value of focal HIFU in select men with localized radiorecurrent clinically significant prostate cancer is needed (clinically significant prostate cancer defined as GG2 or above. GG1 prostate cancer will not be considered clinically significant prostate cancer), both in terms of oncologic and functional outcomes as this patient population is increasing.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patient has elected to undergo focal high intensity focused ultrasound therapy for radiorecurrent prostate cancer
- •Males who are ≥ 18 years of age
- •Eastern Cooperative Oncology Group Performance Status of 0-3
- •A history of prostate cancer treated with radiation therapy +/- hormone therapy
- •MRI or prostate-specific membrane antigen (PSMA) PET region of interest (ROI)
- •Biopsy proven clinically significant prostate cancer (GG2 or above) recurrence within or ipsilateral to the ROI lesion (within 6 months of the MRI/PET).
- •Contralateral grade group 1 (GG1) prostate cancer disease to the ROI
- •PSMA PET negative for metastatic disease (within 6 months of the biopsy)
- •Subjects must not have more than one active malignancy at the time of enrollment (Subjects with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen \[as determined by the treating physician and approved by the PI\] may be included).
- •Written informed consent obtained from the subject and the subject agrees to comply with all the study-related procedures.
Exclusion Criteria
- •Contraindication to high intensity focused ultrasound (latex allergy, absent rectum, prior rectal fistula or significant rectal surgery making insertion of transrectal probe non-feasible or dangerous.)
- •Hormone therapy within 6 months of the screening period (Hormone therapy includes oral (relugolix, abiraterone, enzalutamide, apalutamide, darolutamide, casodex) injections (firmagon, Lupron))
- •History of Inflammatory Bowel Disease actively treated in last 3 years
- •Evidence of ≥ cT3 recurrent disease on imaging
- •Bilateral clinically significant prostate cancer
- •Presence of brachytherapy seeds still implanted
- •Presence of fiduciary markers which directly impede the successful treatment of the lesion of concern, as decided upon by the surgeon upon review of imaging
- •Large Calcification on CT or transrectal ultrasound which, as per the review of the surgeon, limits or hinders a quality high intensity focused ultrasound to the region of interest
- •Urethral stricture disease that has been active over the last 6 months or required further treatment than clean intermittent catheterization
- •No prior radiation therapy for prostate cancer
Outcomes
Primary Outcomes
In-field failure-free survival
Time Frame: 12 months
Evaluate the in-field failure-free survival (IFFFS) of localized radiorecurrent prostate cancer patients receiving focal HIFU treatment at 12 months. IFFFS is defined as the absence of biopsy proven clinically significant prostate cancer in the treated zone.
Secondary Outcomes
- Time from HIFU to whole gland or systemic therapy(3 years)
- Time from HIFU to androgen deprivation therapy onset(3 years)
- Local failure-free survival(12 months)
- Complication rates(12 months)
- Change in quality of life metrics(12 months)